A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792737



Internal ID18827133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19760441..19797524hg38UCSC Ensembl
Innerchr19:19871250..19908333hg19UCSC Ensembl
Innerchr19:19732250..19769333hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3837084
hg1937084
hg1837084
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893168
Supporting Variants
Samples
Known GenesLINC00663, ZNF506
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792737
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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